| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:111859416-111859728 | Common:2; Rare:81 | ||||
| chr3:112086191-112086428 | Common:1; Rare:76 | ||||
| chr3:112561607-112561696 | Rare:34 | ||||
| chr3:112561886-112562162 | Common:1; Rare:85 | ||||
| chr3:113746156-113746476 | Rare:120 | ||||
| chr3:113746966-113747076 | Common:3; Rare:16 | ||||
| chr3:114056475-114056823 | Common:2; Rare:134 | ||||
| chr3:114454928-114455054 | Common:5; Rare:13 | ||||
| chr3:115100253-115100427 | Rare:32 | ||||
| chr3:115147238-115147459 | Common:2; Rare:58 | ||||
| chr3:119468826-119469018 | Rare:73 | ||||
| chr3:119677340-119677519 | Common:1; Rare:63 | ||||
| chr3:120742504-120742777 | Common:2; Rare:77 | ||||
| chr3:121749643-121749993 | Common:1; Rare:80 | ||||
| chr3:121834990-121835234 | Common:3; Rare:80; Clinvar:6; Clinvar (benign):2 |